FDA Inspection 991305 - Allison Medical, Inc. - October 12, 2016

FDA Inspection 991305 for Allison Medical, Inc. on October 12, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 991305 for Allison Medical, Inc. on October 12, 2016. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

21 CFR 820.198(a)

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Record Information

Company

Allison Medical, Inc.

Inspection Date

October 12, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa62a16c-0704-4857-b10e-aaf0555e9333

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